A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17426917



Internal ID22484787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32995193..32995244hg38UCSC Ensembl
chr3:33036685..33036736hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5903612
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17426917
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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